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Towards an integrative approach to the management of myotonic dystrophy type 1
  1. Cynthia Gagnon1,
  2. Luc Noreau3,
  3. Richard T Moxley5,
  4. Luc Laberge1,
  5. Stéphane Jean1,
  6. Louis Richer2,
  7. Michel Perron6,
  8. Suzanne Veillette4,
  9. Jean Mathieu1
  1. 1Neuromuscular Clinic, Centre de Réadaptation en Déficience Physique de Jonquière, Jonquière, Québec, Canada
  2. 2Département des Sciences de l’Education et de Psychologie, Université du Québec à Chicoutimi, Chicoutimi, Québec, Canada
  3. 3Rehabilitation Department, Faculty of Medicine, Université Laval, Québec, Canada
  4. 4Groupe Écobes, Cégep de Jonquière, Jonquière, Québec, Canada
  5. 5Departments of Pediatrics and Neurology, University of Rochester, School of Medicine, Rochester, New York, USA
  6. 6Montreal University Hospital Centre, Montréal, Québec, Canada
  1. Correspondence to:
 Cynthia Gagnon
 Centre de Réadaptation en Déficience Physique de Jonquière, 2230 de l’Hôpital, CP 1200, Jonquière (Québec) G7X 7X2, Canada; cynthia5_gagnon{at}uqac.ca

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Myotonic dystrophy type 1 (DM1) is the most common type of muscular dystrophy in adults. Approximately 60% of individuals report either having difficulty performing or being unable to carry out some activities related to home management, mobility and transportation, work and leisure. Employment, educational level and income are, on average, lower than in the general population. The complexity and variability of disease manifestations in DM1 undoubtedly pose a challenge as regards anticipating all potential problems and developing a plan for health and community management. This article presents a conceptual model for DM1 management as well as a brief discussion of an approach for developing interdisciplinary health and community services.

Myotonic dystrophy type 1 (DM1, OMIM 160900) is the most common type of muscular dystrophy in adults. Its estimated prevalence ranges between 2.1 and 14.3 per 100 000 worldwide, but reaches 189 per 100 000 in the Saguenay–Lac-St-Jean region of the province of Quebec, Canada.1,2 DM1 is an autosomal dominant disease caused by an unstable trinucleotide repeat expansion of the cytosine–thymine–guanine [CTG]n located in the 3′ untranslated region of chromosome 19q13.3.3 DM1 was first described as a muscle disease with gonadal involvement in 1909. Since then, it has been recognised as a multisystemic disorder with various impairments, especially in the muscular, respiratory, cardiac, central nervous, endocrine and ocular systems.4 Typical symptoms of the disease include progressive loss of muscle strength, usually distal to proximal, ptosis, weakness of facial and anterior neck muscles, myotonia, daytime somnolence and cataracts.4 DM1 may also affect the ability of patients to carry out certain daily activities and social roles. Approximately 60% of individuals report either having difficulty performing or being unable to carry out some activities related to home management, mobility and transportation, work and leisure.5 Employment, educational level and income are, on average, lower than in the general population.6

The [CTG]n expansion responsible for DM1 can vary from 50 to over 1000 repetitions, and contributes to a broad range of different phenotypes. Four different clinical phenotypes are recognised in DM1 according to age of onset in conjunction with [CTG]n repeats: congenital, childhood, classic (adult) and late onset forms.7

The diagnosis of DM1 must be considered across the entire age range of a person’s lifespan, and the age at diagnosis will bear management implications according to the severity of the manifestations of the disease. Onset clinical manifestations display great variation between and within each phenotype. While some individuals may consult a neurologist for typical symptoms of severe muscle weakness and myotonia, others may only see an ophthalmologist for cataracts. Anticipation, defined as the earlier onset of symptoms of increasing severity in successive generations within a family, also contributes to the complexity of the clinical manifestations of DM1.2 This complexity not only poses a challenge in establishing a diagnosis of DM1, but also in managing the wide variety of disease manifestations.

Over the past 20 years, recommendations regarding diagnosis, management and care delivery for individuals with genetic disorders have stemmed from the disciplines of medical genetics, paediatrics and neurology.8 Under optimal circumstances, fundamental components in the clinical care of patients with genetic diseases, such as DM1, need to include: (a) appropriate clinical–genetic screening; (b) specific preventive treatments; (c) guidance and anticipation of future care needs; (d) social evaluations to monitor patients for complications; and (e) effective communication and trust with patients and their families. The complexity and variability of disease manifestations in DM1 undoubtedly pose a challenge as regards anticipating all potential problems and developing a plan for health and community management. DM1 patient follow-ups have been described as fragmented, inadequate or even deficient for many patients.4,9 Numerous factors, namely health (multisystemic disease with several disabilities), economic (low income), social (poor social support network) and low educational level, may contribute to this situation. These different factors emphasise the need for a comprehensive management approach in DM1 patient care. This article presents a conceptual model for DM1 management as well as a brief discussion of an approach for developing interdisciplinary health and community services.

DEVELOPMENT OF A CONCEPTUAL FRAMEWORK FOR MANAGEMENT OF MYOTONIC DYSTROPHY

Developing integrated approach plans for managing various aspects of DM1 disease manifestations is important to ensure optimal care. Such an integrated plan can be enhanced through the use of a conceptual framework illustrating the essential items in overall management and, more importantly, the relationship between these different aspects of care. A conceptual approach of this type has been used in diseases such as spina bifida to evaluate its usefulness in integrating management of impairment, disability and restrictions in participation. Such an approach has helped develop standards of care, integrated services and policies.10 In DM1, this conceptual framework may help clinicians: (1) assess all aspects of management at a glance; (2) establish links between several factors influencing social participation; and (3) improve anticipatory guidance through an adequate interdisciplinary health and community management plan.

The traditional medical care model focuses on treatment of impairments. However, more recent models, including the International Classification of Functioning, Disability and Health (ICF), have explained the process of disablement not only in terms of the presence of impairments and disabilities per se, but also in terms of changes in the physical and social environments of affected individuals.11,12 We will discuss briefly two disability models—the ICF and the application of the Disability Creation Process (DCP) model to the management of DM1.

International Classification of Functioning, Disability and Health

The World Health Organisation (WHO) recently issued the final version of the ICIDH-2, now called the ICF.11 Many studies have used the ICF model since its adoption13,17 but there have been some criticisms.14 Firstly, the model kept parts of its linearity, which may lead the disablement process to be viewed as static, sequential and unidirectional. Secondly, environment is not seen as a definite dimension of the model but as a contextual factor, which does not sufficiently emphasise the enormous role of environmental factors.15 As DM1 is overrepresented in the poorer strata of society,6 the influence of environmental factors (community management), such as allocation of healthcare resources or family and social support, must be integrated in the global management plan, and the conceptual framework must recognise the impact of environmental factors on the life of patients with DM1. Thirdly, the possible confusion between the terms activity and participation has been pointed out.14,16 The ICF model has the same list of items for activity and participation domains, and the distinction has to be made by the user. However, Jette et al demonstrated that activity and participation are distinct dimensions and should be treated as such in the WHO model if it is to be used as a scientific model.14 To our knowledge, in neuromuscular disorders, the ICF role has been limited to classifying the impairments and disabilities and has not been used as a model explaining the various consequences (biological, functional and social) of the disease.9

Application of the Disability Creation Process model to DM1

The DCP model (fig 1) resulted from the work conducted by the Quebec Committee on the revision of the WHO International Classification of Impairments, Disabilities and Handicap model.12 The DCP model emerged from a human development model assuming that individuals will experience some type of handicap situation throughout their lives.12 The model has proven useful in populations of patients with spinal cord injury, cerebral palsy as well as in older adults, with and without functional limitations, to document the occurrence of handicap situations and the association with personal characteristics.18–20 The DCP model also serves as a platform for the design and implementation of policies and services for various populations.

Figure 1

 Disability Creation Process model (conceptual scheme).

This article presents the specific health and community aspects of DM1 management according to the DCP model. Our model has sought to use an evidence based approach. Our tables illustrate many internationally accepted clinical characteristics related to this disorder as well as more recent findings. However, the literature on DM1 has been categorised as poor, and available information on the subject is limited. Hence adaptation of the DCP model has solely incorporated factors with a presumed impact on management. Although quality of life is a crucial dimension of rehabilitation, it is not part of the DCP model and will not be discussed, as it will require a paper on its own.

The model includes four domains, which are briefly outlined with clinical examples relevant to DM1.

Risk factors

A risk factor (table 1) is an element related to the individual or the environment that is likely to give rise to a disease or an injury.12 In DM1, the mutation responsible for the disease (number of CTG repeats on chromosome 19q13.3) is a risk factor that partly determines the severity of DM1 symptoms, including muscular impairment (r = 0.46 to 0.51; p<0.05)81 and age of onset (r = −0.82 to 0.57; p<0.01).7,81 Anticipation and the congenital phenotype primarily transmitted by affected women are examples of how the gene defect modulates health outcomes in this disease. In addition, life expectancy is greatly reduced in DM1 patients, particularly in those with early age of onset of disease and the concomitant involvement of proximal muscular weakness.45

Table 1

 Risk factors for myotonic dystrophy type 1 and organic system involvement

Personal factors

A personal factor (tables 1, 2) refers to a person’s intrinsic characteristics, such as, age, sex, sociocultural characteristics, organic systems and capabilities.12 An organic system is defined as a group of biological components sharing a common function, such as the muscular system, with a measurement scale ranging from integrity to impairment. A capability is defined as a person’s potential to accomplish a mental or physical activity. A capability can be measured on a scale ranging from optimal ability to total disability.12 Typically, symptoms become evident during mid-life, but signs of DM1 can be detectable in the first or second decades of life.

Table 2

 Disabilities in myotonic dystrophy type 1

Muscular system and motor activity

Clinical myotonia, facial weakness, atrophy, ptosis, nasal speech and weakness of the sternomastoid and neck flexor muscles, long finger flexors and foot dorsiflexor muscles are the earlier muscular features of DM1. As the disease progresses, other distal muscles of the upper and lower limbs become involved, and later proximal weakness and more severe distal weakness occur.2 The majority of patients with DM1 are able to carry out most basic motor activities but they will perform these tasks more slowly than control subjects, and their performance is likely to deteriorate over time.68,82

Nervous system and intellectual and behavioural capabilities

Intellectual functioning in adult DM1 patients falls within the range of the normal population.83 In many cases, DM1 patients have great difficulties with abstraction and new concept formation, resulting in a tendency to rigidity and perseveration. The incidence of anxiety disorders and depression is also higher in this population.84 Although the physiopathology of hypersomnia remains unclear, excessive daytime sleepiness is a prominent feature of DM1,30 sometimes preceding muscular involvement by many years.85 Symptoms of severe sleepiness may markedly impair social or occupational functions.86 Fatigue is frequently reported on clinical assessments in DM187; its diagnosis and evaluation are rarely if ever specifically addressed.88 Emotional factors and personality as well as education, facial appearance, nasal voice, introversion, apathy and excessive daytime sleepiness create the popular label of a lower intelligence. This label in turn tends to influence DM1 patients in their learning or social interactions.89

Ocular system

Cataracts may be the only presenting symptom in the late onset form of DM1. The presence of cataracts is almost always present in adults but rare under the age of 10 years.2

Digestive system

Digestive symptoms, including abdominal pain and diarrhoea, may disrupt daily life and prevent participation in many social activities. Gastrointestinal disturbances are the most disabling impairment in 25% of patients.33

Respiratory system

Involvement of the upper airway and expiratory muscles may occur early in the course of DM1.35 Later in the evolution of the disease, the weakness of respiratory muscles decreases the vital capacity and increases the risk of alveolar hypoventilation.35 There is an increased risk of perioperative pulmonary complications.65

Cardiovascular system

Cardiac arrhythmias and conduction defects are well known and frequent complications of DM1, and they can lead to sudden death. Pacemaker implantation is necessary in approximately 5% of patients. The risk of conduction disturbances and sudden death increases with duration of the disease and age, but cases of exercise induced tachycardias have been reported in childhood.90

Endocrine system

Hypogonadism is the most frequent endocrine abnormality in DM1 patients.84 In adult males, markedly elevated follicle stimulating hormone levels and moderately low testosterone levels are frequently observed. Significant reductions in serum adrenal androgen levels are often observed in affected patients, and these deficiencies may contribute to cognitive impairment.46,50

Reproductive system

Pregnancy in women with the adult form of DM1 is often accompanied by obstetric complications. The risk of perinatal loss is approximately 15% compared with 1.9% in the reference population.67

Environmental factors

An environmental factor (table 3) is defined as a physical or social dimension that determines a society’s organisation and context. Environmental social factors include political/economic factors and sociocultural factors. Physical environmental factors are divided into the nature group (weather, time, etc.) and the development group (architecture, vehicles). Environmental factors are assessed on a qualitative scale ranging from being an optimal facilitator to a total obstacle. A facilitator helps while an obstacle hinders the performance of life habits, in interaction with personal factors.12

Table 3

 Environmental factors in myotonic dystrophy type 1

Poverty and social exclusion are frequently observed social environmental factors in DM1.6 A much larger proportion of affected individuals (43.6%) than in the general population (12.2%) depend on social welfare, which places them below the poverty line.6 Employment opportunities are also limited by their educational level. More than half of the DM1 population has no high school diploma.80 It has been suggested that the progressive social deterioration of DMI families occurs over several generations as more severe forms of the disease appear.

Because DM1 is still relatively unknown among medical and paramedical resources, the provision of healthcare and community services is underdeveloped. Care is inconsistent, problematic and in many areas only given yearly, at best.4,30 A multidisciplinary neuromuscular clinic is rarely the main care provider for the day-to-day management of this patient population.

Social participation

Social participation (table 4) is described and assessed using the concept of life habits, which are defined as daily activities or social roles valued by the person according to his/her sociocultural context and characteristics (age, sex, sociocultural identity, etc). The DCP model assumes that social participation is the product of the interaction between personal and environmental factors. The accomplishment of life habits ranges from full social participation to a total handicap situation.12

Table 4

 Life Habits in myotonic dystrophy type 1

In DM1, various life habits are known to be disrupted in one way or another in the congenital, childhood and adult forms of the disease. Only a small percentage of this population is able to maintain an active and fulfilling life.5 In the adult form, daily activities related to mobility and nutrition are often the first to be disrupted. With the progression of muscular involvement, patients usually need a wheelchair for short or long distances and have considerable difficulty in carrying out their daily living activities.

With respect to the accomplishment of social roles, the clinical picture often seen in the adult form is that of a sedentary person with few relationships except for family members. Participation in the community is severely restricted. These individuals typically have left school early, and have rarely held a steady job or taken part in community activities. Fulfilment of their daily responsibilities is often difficult, even more so when several family members are affected by DM1. A common situation is that of an affected mother with a severely affected child. She is not able to cope with the daily care of her family and is confronted with the progressive deterioration of their social participation.

The present conceptual framework illustrated the management elements needed to improve care of this underserved population. Potential solutions for optimal organisation and planning of services are discussed below.

DEVELOPMENT OF A COMPREHENSIVE HEALTH AND COMMUNITY MANAGEMENT FRAMEWORK FOR DM1

From physician oriented outcomes to patient oriented outcomes

Health supervision has now been established as part of the clinical practice’s foundation and is important in terms of performing appropriate screenings, applying specific preventive measures and developing a relationship with families.8 The mainstay of care is anticipatory guidance and monitoring for treatable complications. Literature and clinical experiences worldwide clearly demonstrate that DM1 patients and their families are provided with suboptimal health management, including insufficient anticipatory guidance. The multiplicity and variability of the disease manifestations, the health professionals’ limited knowledge of DM1, time constraints and difficulty in targeting guidance on the topics of greatest concern to patients are some of the factors explaining this observation.

Integrating all of the clinical manifestations into a conceptual framework is not sufficient, as each aspect clearly does not deserve the same attention in DM1 health management. Some assessment protocols focusing on impairments have already been developed.91,92 Clinical experience suggests that myotonia and muscle strength, although important to assess, are not the main concern of DM1 patients.4 The resulting difficulties in daily activities and access to services that help overcome them, which are often not properly addressed, are far more important to patients and their families. When properly identified and included in a continuum of care, improvement in dealing with health, social and family environmental factors can partly counterbalance existing impairments and disabilities, and prevent the development of handicap situations in life habits. Development and implementation of environmental facilitators, such as access to high quality healthcare and community services, can be a key concept in support provided to people with DM1. When assessment moves from a focus on impairment to a focus on social participation, the integration of an interdisciplinary team into the health management programme becomes mandatory.

Community based case management: a model to be developed in DM1

In order to implement a health management programme, service development needs to be carefully reviewed. A health management programme must provide support to both the patient and family through an interdisciplinary team, which includes genetic and medical resources as well as community resources.91 Such programmes needs to be concerned not only with treating patients during discrete care episodes but also with providing high quality care across the continuum. It is common knowledge that currently available healthcare resources in many countries do not permit appropriate evaluation and follow-up by an interdisciplinary team. In Canada, and probably in many other countries, the solution may lie in an organisation of care more centred on the nursing staff, with correspondingly increased responsibility in the evaluation and referral procedures related to healthcare and community resources.92 A community based nursing case management programme, as part of a health management programme, has been developed as a method of care delivery for several chronic diseases.93 The nurse is able to act as a case manager to help achieve goals set by the interdisciplinary team, namely by planning follow-up individual assessments for service referrals, needed services and resource identification, and strengthening the links between resources and patients, thus ensuring a continuum of care.94 Services needed by DM1 patients include genetic counselling, anticipatory guidance, referrals to medical and healthcare professionals, patient and family support within the healthcare system and referral to community services. Practically, it means moving from a single physician management approach to interdisciplinary management coordinated by a nurse. Such measures may also enable the release of medical staff to concentrate on more specialised areas of clinical genetic services, such as diagnosis.92 Before such an approach can be implemented, research is needed to develop appropriate health management protocols and an intervention decision tree to support the nurse’s evaluation and assess the validity and efficacy of this community based nursing case management programme.

CONCLUSION

Myotonic dystrophy is a complex disease that needs to be addressed with a comprehensive conceptual framework, which simultaneously considers several aspects of the individual’s life in order to help the person achieve optimal social participation according to his/her expectations.

The DCP model offers a unique perspective to help understand the reasons and processes explaining why social participation is disrupted among many DM1 patients. The close relationships between some personal factors, such as fatigue, motivation and decreased strength, must be seen in relation to their interaction with environmental factors and impact on different aspects of social participation. The model not only points out impairments and disabilities, but also the role of environmental factors, such as access to healthcare, family support and income, as possible explanations for their low social participation. A health management programme based on this conceptual framework needs to be developed in order to improve services provided to this underserved population. Within such a health management programme, a community based nursing case management programme may be an interesting model to develop. The most important message conveyed by the DCP model is to shift DM1 management from traditional physician oriented outcomes at the medical clinic to patient oriented outcomes in the community, where there are tremendous opportunities to improve individuals’ social participation.

Acknowledgments

This research was supported by the Neuromuscular Partnership Program of Muscular Dystrophy Canada, the Canadian Institutes of Health Research (CIHR) (#MOP49556) and ECOGENE-21, a research programme in community genetics and genomics supported by the Canada Research Chairs Program and the CIHR (#CAR43283). CG holds a PhD Scholarship from the Canadian Institutes of Health Research.

Myotonic dystrophy type 1 (DM1) is the most common type of muscular dystrophy in adults. Approximately 60% of individuals report either having difficulty performing or being unable to carry out some activities related to home management, mobility and transportation, work and leisure. Employment, educational level and income are, on average, lower than in the general population. The complexity and variability of disease manifestations in DM1 undoubtedly pose a challenge as regards anticipating all potential problems and developing a plan for health and community management. This article presents a conceptual model for DM1 management as well as a brief discussion of an approach for developing interdisciplinary health and community services.

REFERENCES

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Footnotes

  • Published Online First 20 April 2007

  • Competing interests: None.

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